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Details
Link-It Detail - Disease - Ectropion
Debug Stats
  • ### Total Build Time: 49 ms 26.956 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 316 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 286 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 551 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.490 KB
  • CONCEPT_RELATIONSHIPS gt=31 ms Completed: 31 ms rowSize= 12.311 KB
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 10.667 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.144 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Ectropion C0013592
Definition (1)
The turning outward (eversion) of the edge of the eyelid, resulting in the exposure of the palpebral conjunctiva. (Dorland, 27th ed)
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Eyelid Diseases C0015423
Ancestral Roots
RootRoot Plus OneDepthParent
img Eye Diseases C0015397img Eyelid Diseases C00154233img Eyelid Diseases C0015423
Relationships (29)

Relation Types:
diso_​to_​anat : 4
diso_​to_​diso : 25


Relationships:
none : 12
classifies : 1
isa : 8
mapped_​to : 7
used_​for : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT26img Eyelid structure C0015426
DISO_to_ANAT23img Eyelid structure C0015426
DISO_to_DISO12img Cicatrix C2004491
DISO_to_DISO9img ENTROPION C0014390
DISO_to_DISO9img Facial Paralysis C0015469
DISO_to_DISO8img Cicatrix C2004491
DISO_to_DISO8img chemically induced C0007994
DISO_to_DISO7img ENTROPION C0014390
DISO_to_ANAT6img Surgical Flaps C0038925
DISO_to_ANAT5img Surgical Flaps C0038925
DISO_to_DISO5img Complication Aspects C1171258
DISO_to_DISO5img EYELID NEOPL C0015424
DISO_to_DISOused_forimg A-760-766 DISORDERS OF THE EYELIDS C0015423
DISO_to_DISOisaimg Age-related ectropion C0155193
DISO_to_DISOmapped_toimg BCD SYNDROME C1861536
DISO_to_DISOisaimg Cicatricial ectropion C0155196
DISO_to_DISOisaimg Congenital ectropion C0266578
DISO_to_DISOmapped_toimg ECTROPION C0013592
DISO_to_DISOisaimg Ectropion of lower lid C0521736
DISO_to_DISOisaimg Entropion - ectropion combination C0521734
DISO_to_DISOmapped_toimg ICHTHYOSIS WITH ALOPECIA, ECLABION, ECTROPION, AND MENTAL RETARDATION C1855788
DISO_to_DISOmapped_toimg Lower eyelid tarsal ectropion C1443283
DISO_to_DISOisaimg Mechanical ectropion C0155194
DISO_to_DISOmapped_toimg Medial ectropion C1689997
DISO_to_DISOclassifiesimg Other disease of eye C0497217
Genes (12)

Species:
human : 12
SpeciesGeneGeneIdGene NameEvidence
HumanABHD551099abhydrolase domain containing 5
img OMIM, Score=1000, UMLKSK CUI: C0013592
HumanABCA1226154ATP-binding cassette, sub-family A (ABC1), member 12
img OMIM, Score=833, UMLKSK CUI: C0013592
HumanXPA7507xeroderma pigmentosum, complementation group A
img OMIM, Score=1000, UMLKSK CUI: C0013592
HumanSAT16303spermidine/spermine N1-acetyltransferase 1
img OMIM, Score=1000, UMLKSK CUI: C0013592
HumanPOLH5429polymerase (DNA directed), eta
img OMIM, Score=1000, UMLKSK CUI: C0013592
HumanNF14763neurofibromin 1
img GENERIF, Score=1000, Pubmed Id: 15627836, UMLKSK CUI: C0013592
HumanITGB43691integrin, beta 4
img OMIM, Score=1000, UMLKSK CUI: C0013592
HumanITGA63655integrin, alpha 6
img OMIM, Score=1000, UMLKSK CUI: C0013592
HumanERCC62074excision repair cross-complementing rodent repair deficiency, complementation group 6
img OMIM, Score=1000, UMLKSK CUI: C0013592
HumanERCC22068excision repair cross-complementing rodent repair deficiency, complementation group 2
img OMIM, Score=1000, UMLKSK CUI: C0013592
HumanDDB21643damage-specific DNA binding protein 2, 48kDa
img OMIM, Score=1000, UMLKSK CUI: C0013592
HumanABCA119ATP-binding cassette, sub-family A (ABC1), member 1
img OMIM, Score=1000, UMLKSK CUI: C0013592
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0013592Ectropion0self